A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579100



Internal ID21527576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6978007..6978219hg38UCSC Ensembl
chr4:6979734..6979946hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137781
SamplesNA19238
Known GenesTBC1D14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579100
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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